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Sigma-Aldrich

7-Bromindol

96%

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About This Item

Empirische Formel (Hill-System):
C8H6BrN
CAS-Nummer:
51417-51-7
Molekulargewicht:
196.04
MDL-Nummer:
MFCD00799492
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24870925
NACRES:
NA.22

Assay

96%

Form

solid

mp (Schmelzpunkt)

41-44 °C (lit.)

SMILES String

Brc1cccc2cc[nH]c12

InChI

1S/C8H6BrN/c9-7-3-1-2-6-4-5-10-8(6)7/h1-5,10H

InChIKey

RDSVSEFWZUWZHW-UHFFFAOYSA-N

Verwandte Kategorien

Allgemeine Beschreibung

7-Bromoindole is a 7-substituted indole derivative. Its synthesis from 7-bromoindole-2-carboxylic acid has been reported. It has been reported to reduce the production of staphyloxanthin in Staphylococcus aureus.

Anwendung

7-Bromoindole may be used in the synthesis of the following:
  • indole
  • dyestuffs
  • 8-bromocarboline

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

235.4 °F - closed cup

Flammpunkt (°C)

113 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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Sigma-Aldrich

M51490

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4-Cyanoindol 97%

Sigma-Aldrich

645532

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Jin-Hyung Lee et al.
Applied microbiology and biotechnology, 97(10), 4543-4552 (2013-01-16)
Human pathogens can readily develop drug resistance due to the long-term use of antibiotics that mostly inhibit bacterial growth. Unlike antibiotics, antivirulence compounds diminish bacterial virulence without affecting cell viability and thus, may not lead to drug resistance. Staphylococcus aureus
Zhiqian Wang et al.
Tetrahedron letters, 53(5), 477-479 (2012-05-01)
A novel MCAP-cycloaddition sequence has been applied to the facile synthesis of β-carboline intermediates to gain rapid access to novel derivatives of yohimbine-like and corynanthe-like compounds that may be easily diversified by cross-coupling reactions and N-derivatizations to generate small compound
The structure of monobrominated ethyl indole-3-carboxylate and the preparation of 7-bromoindole.
Leggetter BE and Brown RK.
Canadian Journal of Chemistry, 38(9), 1467-1471 (1960)
Total synthesis of indoles from Tricholoma species via Bartoli/heteroaryl radical methodologies.
A Dobbs
The Journal of organic chemistry, 66(2), 638-641 (2001-06-30)
J Y Kim et al.
Letters in applied microbiology, 41(2), 163-168 (2005-07-22)
To establish multicomponent phenol hydroxylases (mPHs) as novel biocatalysts for producing dyestuffs and hydroxyindoles such as 7-hydroxyindole (7-HI) from indole and its derivatives. We have isolated Pseudomonas sp. KL33, which possesses a phenol degradation pathway similar to that found in
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